Clinical Research Manager

TFS HealthScience is a leading mid-sized Contract Research Organization (CRO) dedicated to partnering with biotechnology and pharmaceutical companies throughout their clinical development journey. Our Clinical Operations team led by industry experts combines the full-service capabilities and global reach of a large CRO with the flexibility and personal approach of a mid-sized CRO.

As a member of our SRS team you will be fully dedicated to a single sponsor based in the United States. This is a contract-based position.

Responsibilities:

• Develop and maintain strong relationships with key personnel at clinical trial sites including principal investigators site coordinators and other site staff.
• Serve as a bridge between the sponsor and clinical trial sites ensuring clear and timely communication of study protocols updates and key information.
• Conduct Monitoring Oversight Visits and regular site engagement activities to ensure high-quality trial execution.
• Design customized site-level engagement plans to help drive enrollment and support timely patient recruitment.
• Collaborate with CRO CRAs and Medical Science Liaisons to identify mitigate and resolve site-level challenges.
• Participate in feasibility and site qualification visits collaborating with CRO representatives.
• Represent the sponsor at local and regional patient advocacy or support group meetings when needed.
• Track and report site engagement activities enrollment status and performance metrics.

Travel Requirements:

• This is a very high travel position with at least 75% travel.
• Sites will primarily be located in the Central USA region though travel outside this area may occasionally be required.

Requirements:

• Bachelors degree in a relevant field (life sciences nursing healthcare management).
• Proven experience in clinical research and site relationship management.
• Excellent communication and interpersonal skills.
• Proactive problem-solving abilities.
• Strong organizational and project management skills.
• Solid understanding of GCP and regulatory requirements.
• Must reside within 30-45 minutes of one of the following airports: Dallas (DFW) Houston (IAH) Chicago (ORD) Minneapolis (MSP) or Detroit (DTW).

Contract Type:
0.7 FTE

Therapeutic areas: Rare diseases and autoimmune disorders.